Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy

por Ngo, Michael H., Borowska-Fielding, Joanna, Heathcote, Godfrey, Nejat, Sara, Kelly, Melanie E., McMaster, Christopher R., Robitaille, Johane M.
Publicado 2016

Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9

por Prykhozhij, Sergey V, Fuller, Charlotte, Steele, Shelby L, Veinotte, Chansey J, Razaghi, Babak, Robitaille, Johane M, McMaster, Christopher R, Shlien, Adam, Malkin, David, Berman, Jason N
Publicado 2018

Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9

por Prykhozhij, Sergey V, Fuller, Charlotte, Steele, Shelby L, Veinotte, Chansey J, Razaghi, Babak, Robitaille, Johane M, McMaster, Christopher R, Shlien, Adam, Malkin, David, Berman, Jason N
Publicado 2018

Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4

por van der Ende, Sarah R., Meyers, Benjamin S., Capasso, Jenina E., Sasongko, Mario, Yonekawa, Yoshihiro, Pihlblad, Matthew, Huey, Jennifer, Bedoukian, Emma C., Krantz, Ian D., Ngo, Michael H., McMaster, Christopher R., Levin, Alex V., Robitaille, Johane M.
Publicado 2022